NDC | 50845-0238-1, 50845-0238-2 |
Set ID | 534d70a8-f224-40e6-881f-d34ece9f6523 |
Category | HUMAN OTC DRUG LABEL |
Packager | Liddell Laboratories, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number |
- ACTIVE INGREDIENTS:
-
USES:
May temporarily relieve the ill effects - not the therapeutic effects - of oral or injected vaccines. Children and adults may expect temporary relief from symptoms such as:
• minor fever
• pain
• redness
• weakness
• lack of energy
• swelling**
**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
-
WARNINGS:
Do not use if you have ever had an allergic reaction to this product or any of its ingredients.
Ask a doctor before use if excessive redness or swelling is present.
Stop use and ask a doctor if symptoms persist, worsen or if new symptoms occur.
Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.
If pregnant or breast feeding, ask a doctor before using product.
Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.
Other Information:
Store at room temperature.
- KEEP OUT OF REACH OF CHILDREN:
-
DIRECTIONS:
Adults & children over 12: Place 15 drops under the tongue 3 times per day.
Children 2 to 12: Administer 1 drop under the tongue per year of age, 3 times per day.
Children 1 and under: Administer 1 drop under the tongue, 3 times per day.
For recent vaccinations, use daily for two weeks. For old vaccinations, use daily for one month. Consult a physician for use in children under 12.
-
INDICATIONS:
May temporarily relieve the ill effects - not the therapeutic effects - of oral or injected vaccines. Children and adults may expect temporary relief from symptoms such as:
• minor fever
• pain
• redness
• weakness
• lack of energy
• swelling**
**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
- INACTIVE INGREDIENTS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY:
-
INGREDIENTS AND APPEARANCE
VACCINES
arnica montana, mercurius corrosivus, sulphur iodatum, thuja occidentalis, urtica urens liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50845-0238 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA 3 [hp_X] in 1 mL MERCURIC CHLORIDE (UNII: 53GH7MZT1R) (MERCURIC CATION - UNII:ED30FJ8Y42) MERCURIC CHLORIDE 200 [hp_C] in 1 mL SULFUR IODIDE (UNII: L6L8KA2AA0) (SULFUR IODIDE - UNII:L6L8KA2AA0) SULFUR IODIDE 200 [hp_C] in 1 mL THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786) (THUJA OCCIDENTALIS LEAF - UNII:0T0DQN8786) THUJA OCCIDENTALIS LEAF 200 [hp_C] in 1 mL URTICA URENS (UNII: IHN2NQ5OF9) (URTICA URENS - UNII:IHN2NQ5OF9) URTICA URENS 3 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50845-0238-2 1 in 1 CARTON 03/06/2018 1 NDC:50845-0238-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 03/06/2018 Labeler - Liddell Laboratories, Inc. (832264241) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(50845-0238) , api manufacture(50845-0238) , label(50845-0238) , pack(50845-0238)